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Single seeds exhibit transcriptional heterogeneity during secondary dormancy induction

Seeds are highly resilient to the external environment, which allows plants to persist in unpredictable and unfavorable conditions. Some plant species have adopted a bet-hedging strategy to germinate a variable fraction of seeds in any given condition, and this could be explained by population-based...

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Autores principales: Krzyszton, Michal, Yatusevich, Ruslan, Wrona, Magdalena, Sacharowski, Sebastian P, Adamska, Dorota, Swiezewski, Szymon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438484/
https://www.ncbi.nlm.nih.gov/pubmed/35670742
http://dx.doi.org/10.1093/plphys/kiac265
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author Krzyszton, Michal
Yatusevich, Ruslan
Wrona, Magdalena
Sacharowski, Sebastian P
Adamska, Dorota
Swiezewski, Szymon
author_facet Krzyszton, Michal
Yatusevich, Ruslan
Wrona, Magdalena
Sacharowski, Sebastian P
Adamska, Dorota
Swiezewski, Szymon
author_sort Krzyszton, Michal
collection PubMed
description Seeds are highly resilient to the external environment, which allows plants to persist in unpredictable and unfavorable conditions. Some plant species have adopted a bet-hedging strategy to germinate a variable fraction of seeds in any given condition, and this could be explained by population-based threshold models. Here, in the model plant Arabidopsis (Arabidopsis thaliana), we induced secondary dormancy (SD) to address the transcriptional heterogeneity among seeds that leads to binary germination/nongermination outcomes. We developed a single-seed RNA-seq strategy that allowed us to observe a reduction in seed transcriptional heterogeneity as seeds enter stress conditions, followed by an increase during recovery. We identified groups of genes whose expression showed a specific pattern through a time course and used these groups to position the individual seeds along the transcriptional gradient of germination competence. In agreement, transcriptomes of dormancy-deficient seeds (mutant of DELAY OF GERMINATION 1) showed a shift toward higher values of the germination competence index. Interestingly, a significant fraction of genes with variable expression encoded translation-related factors. In summary, interrogating hundreds of single-seed transcriptomes during SD-inducing treatment revealed variability among the transcriptomes that could result from the distribution of population-based sensitivity thresholds. Our results also showed that single-seed RNA-seq is the method of choice for analyzing seed bet-hedging-related phenomena.
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spelling pubmed-94384842022-09-06 Single seeds exhibit transcriptional heterogeneity during secondary dormancy induction Krzyszton, Michal Yatusevich, Ruslan Wrona, Magdalena Sacharowski, Sebastian P Adamska, Dorota Swiezewski, Szymon Plant Physiol Focus Issue on Evolution of Plant Structure and Function Seeds are highly resilient to the external environment, which allows plants to persist in unpredictable and unfavorable conditions. Some plant species have adopted a bet-hedging strategy to germinate a variable fraction of seeds in any given condition, and this could be explained by population-based threshold models. Here, in the model plant Arabidopsis (Arabidopsis thaliana), we induced secondary dormancy (SD) to address the transcriptional heterogeneity among seeds that leads to binary germination/nongermination outcomes. We developed a single-seed RNA-seq strategy that allowed us to observe a reduction in seed transcriptional heterogeneity as seeds enter stress conditions, followed by an increase during recovery. We identified groups of genes whose expression showed a specific pattern through a time course and used these groups to position the individual seeds along the transcriptional gradient of germination competence. In agreement, transcriptomes of dormancy-deficient seeds (mutant of DELAY OF GERMINATION 1) showed a shift toward higher values of the germination competence index. Interestingly, a significant fraction of genes with variable expression encoded translation-related factors. In summary, interrogating hundreds of single-seed transcriptomes during SD-inducing treatment revealed variability among the transcriptomes that could result from the distribution of population-based sensitivity thresholds. Our results also showed that single-seed RNA-seq is the method of choice for analyzing seed bet-hedging-related phenomena. Oxford University Press 2022-06-07 /pmc/articles/PMC9438484/ /pubmed/35670742 http://dx.doi.org/10.1093/plphys/kiac265 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Focus Issue on Evolution of Plant Structure and Function
Krzyszton, Michal
Yatusevich, Ruslan
Wrona, Magdalena
Sacharowski, Sebastian P
Adamska, Dorota
Swiezewski, Szymon
Single seeds exhibit transcriptional heterogeneity during secondary dormancy induction
title Single seeds exhibit transcriptional heterogeneity during secondary dormancy induction
title_full Single seeds exhibit transcriptional heterogeneity during secondary dormancy induction
title_fullStr Single seeds exhibit transcriptional heterogeneity during secondary dormancy induction
title_full_unstemmed Single seeds exhibit transcriptional heterogeneity during secondary dormancy induction
title_short Single seeds exhibit transcriptional heterogeneity during secondary dormancy induction
title_sort single seeds exhibit transcriptional heterogeneity during secondary dormancy induction
topic Focus Issue on Evolution of Plant Structure and Function
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438484/
https://www.ncbi.nlm.nih.gov/pubmed/35670742
http://dx.doi.org/10.1093/plphys/kiac265
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